Regulatory Affairs Specialist 3 - Medical Device IVD
for ensuring regulatory compliance and supporting global market access for in vitro diagnostic (IVD) products. It involves...
for ensuring regulatory compliance and supporting global market access for in vitro diagnostic (IVD) products. It involves...
as in-vitro diagnostics. But we don’t stop at healthcare;our Non-Destructive Testing (NDT) team harnesses advanced radiography...
diagnostic imaging, enterprise imaging, endoscopic and surgical imaging, as well as in-vitro diagnostics. But we don’t stop...
and external work performed to develop our in vitro diagnostics is in compliance with Good Clinical Practice, applicable regulatory... understanding of Good Clinical Practices is required. 4+ years working in the In Vitro Diagnostic or Medical Device Industry...
integrity, and patient safety. About RDI RDI is a nimble, full-service CRO focused on accelerating in vitro diagnostic (IVD...
and other International In vitro diagnostic regulations and standards. At least three to five years of pre-market regulatory experience... regulatory clearance/approvals for In vitro diagnostic products required. Must be able to work well in team environment...
, and interpret genome editing tools development experiments, including molecular, biochemical, in vitro, and cell analyses;Plan...
Antibody team. You will contribute to the identification of potential therapeutic antibodies, the in vitro characterization... might include: Designing and optimizing in-vitro protein or cell-based immunoassays, including but not limited to flow cytometry...
evaluation, antibody optimization, library design, or developability prediction. Generate and interpret data from in vitro and ex...
market compliance experience in in-vitro diagnostics and/or medical device industry. At least 4 years of experience managing... of experience requirement. Skills & Capabilities: Working knowledge of current in vitro diagnostics regulations, guidances...